50799492-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24086
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 31929680-T-G

50799665-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24086
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 31929507-C-T

50799967-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24086
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 31929212-T-C

50800062-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24086
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 31929102-G-T

50800500-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24086
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 31928737-T-C

50800585-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24086
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 31928654-T-C

50800718-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24086
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 31928523-A-G

50804070-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24086
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 31927844-T-C

50804262-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24086
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 31927310-G-A

50804356-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24086
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 31927245-C-T

50804661-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24086
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 31926937-G-A

http://identifiers.org/hco/10/GRCh38#50804709-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24086
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#31926880-C-A

50804709-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24086
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 31926880-C-G

50804861-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24086
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 31926727-A-G

50804916-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24086
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 31926678-G-T

50805008-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24086
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 31926586-G-A

50805097-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24086
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 31926495-A-G

50805275-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24086
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 31926302-A-G

50805642-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24086
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 31926019-A-G

50805648-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24086
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 31926013-G-A

50805648-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24086
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 31926013-G-T

50805714-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24086
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 31925950-T-C

50805714-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24086
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 31925950-T-G

50805762-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24086
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 31925863-T-C

50805877-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24086
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 31925735-A-G

50805926-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24086
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 31925689-T-C

50805989-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24086
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 31925583-G-C

50806022-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24086
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 31925553-A-G

50806064-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24086
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 31925512-C-T

50806129-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24086
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 31925448-G-A

50806129-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24086
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 31925448-G-T

50806241-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24086
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 31925337-G-C

50806246-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24086
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 31925332-G-A

50806246-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24086
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 31925332-G-T

http://identifiers.org/hco/10/GRCh38#50806277-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24086
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#31925304-C-A

50806277-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24086
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 31925304-C-T

50806333-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24086
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_variant, splice_donor_variant
orthologous variants: 31925252-T-A

http://identifiers.org/hco/10/GRCh38#50806340-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24086
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#31925245-C-A

50806455-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24086
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 31925159-T-C

50806466-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24086
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 31925148-T-C

50806494-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24086
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 31925119-G-T

http://identifiers.org/hco/10/GRCh38#50806496-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24086
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#31925117-C-A

50806496-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24086
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 31925117-C-T

50806584-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24086
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 31925045-T-A

50806608-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24086
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 31925021-G-T

50806704-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24086
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 31924930-T-C

50806760-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24086
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 31924877-G-C

50806760-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24086
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 31924877-G-T

50806913-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24086
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31924724-G-A

50806946-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24086
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31924691-T-C

50806970-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24086
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31924666-T-A

50807031-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24086
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31924608-A-T

50809646-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24086
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31923528-A-T

50809660-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24086
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31923514-A-G

50809847-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24086
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31923392-C-T

50809876-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24086
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31923363-G-A

50809911-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24086
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 31923318-G-A

50809942-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24086
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 31923284-C-T

50810150-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24086
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31923107-G-A

50810150-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24086
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31923107-G-T

50810174-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24086
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31923052-G-T

50810182-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24086
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31923043-A-T

50810192-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24086
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31923033-T-C

50810192-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24086
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31923033-T-G

50810233-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24086
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31922993-A-G

50810357-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24086
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31922877-T-C

50810432-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24086
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31922808-T-C

50810444-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24086
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31922787-A-G

50810446-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24086
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31922785-G-C

50810484-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24086
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31922751-A-G

50810484-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24086
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31922751-A-T

http://identifiers.org/hco/10/GRCh38#50810840-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24086
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#31922699-C-A

http://identifiers.org/hco/10/GRCh38#50810871-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24086
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#31922670-A-C

http://identifiers.org/hco/10/GRCh38#50810903-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24086
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#31922638-C-A

50810903-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24086
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31922638-C-T

http://identifiers.org/hco/10/GRCh38#50810948-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24086
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#31922595-C-A

50810951-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24086
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31922592-C-T

http://identifiers.org/hco/10/GRCh38#50810976-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24086
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#31922567-A-C

50810994-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24086
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31922549-G-A

50810994-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24086
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31922549-G-T

50811123-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24086
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 31922415-C-T

50811130-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24086
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 31922408-T-C

http://identifiers.org/hco/10/GRCh38#50811215-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24086
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#31922324-A-C

50811215-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24086
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31922324-A-G

http://identifiers.org/hco/10/GRCh38#50811257-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24086
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#31922283-A-C

50811282-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24086
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31922263-G-A

50811282-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24086
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31922263-G-C

50811282-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24086
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31922263-G-T

50812115-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24086
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31914241-T-C

50812136-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24086
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31914224-G-A

50812136-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24086
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31914224-G-T

http://identifiers.org/hco/10/GRCh38#50812265-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24086
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#31914097-C-A

50812265-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24086
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31914097-C-T

50812317-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24086
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31914045-A-G

50812336-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24086
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31914030-C-T

http://identifiers.org/hco/10/GRCh38#50812732-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24086
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#31913814-A-C

50812793-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24086
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31913752-T-G

50812798-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24086
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31913748-C-T

50812827-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24086
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31913721-A-G

50813054-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24086
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31913447-G-C

http://identifiers.org/hco/10/GRCh38#50813147-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24086
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#31913356-A-C

http://identifiers.org/hco/10/GRCh38#50813343-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24086
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#31913170-A-C

50813568-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24086
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31912451-G-C

50813708-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24086
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31912346-T-C

http://identifiers.org/hco/10/GRCh38#50813709-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24086
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#31912345-C-A

50813774-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24086
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31912300-G-A

50813774-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24086
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31912300-G-T

50813939-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24086
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 31912149-A-T

50814169-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24086
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31911919-G-T

50814312-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24086
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31911790-A-G

50814429-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24086
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31911682-G-A

50814911-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24086
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31911205-C-T

http://identifiers.org/hco/10/GRCh38#50814941-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24086
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#31911175-A-C

50814941-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24086
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31911175-A-G

50815511-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24086
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31910616-G-A

50815629-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24086
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31910492-A-G

50815707-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24086
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31910429-A-G

50815743-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24086
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31910394-G-T

50815941-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24086
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31910193-G-A

50815946-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24086
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31910188-T-G

50815954-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24086
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31910148-G-T

50816158-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24086
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 31909944-G-A

50816318-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24086
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 31909792-A-T

http://identifiers.org/hco/10/GRCh38#50816327-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24086
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#31909783-A-C

50816328-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24086
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 31909782-C-T

50816417-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24086
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 31909721-G-A

50816417-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24086
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 31909721-G-T

50816438-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24086
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 31909699-G-A

50816438-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24086
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 31909699-G-T

50816439-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24086
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 31909698-A-G

50816548-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24086
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31909611-T-G

50816569-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24086
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31909590-G-T

50816609-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24086
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31909547-T-C

50816683-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24086
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31909487-T-A

50816978-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24086
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31909243-G-A

50818540-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24086
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31906898-G-A

50818570-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24086
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31906868-T-G

50818926-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24086
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31906547-C-G

50818926-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24086
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31906547-C-T

50818942-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24086
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31906532-T-C

50819038-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24086
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31906427-G-A

50819405-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24086
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31906123-G-A

50819614-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24086
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31905876-G-C

50819732-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24086
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31905772-G-C

50820009-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24086
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31905503-G-T

50820147-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24086
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31905360-A-G

50820229-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24086
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31905183-C-G

50820229-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24086
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31905183-C-T

50820411-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24086
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31904754-T-C

50820411-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24086
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31904754-T-G

50820414-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24086
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31904751-A-T

50820432-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24086
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31904733-T-C

50820490-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24086
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31904665-G-A

50820490-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24086
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31904665-G-T

50820515-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24086
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31904640-A-G

50820545-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24086
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 31904610-A-T

50820591-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24086
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 31904564-T-G

50820660-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24086
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31904499-G-C

50820660-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24086
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31904499-G-T

50820671-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24086
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31904488-G-T

50820757-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24086
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31904428-C-T

50820784-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24086
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31904405-G-C

50820784-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24086
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31904405-G-T

50820898-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24086
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31904305-G-A

50820906-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24086
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31904297-T-C

50820940-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24086
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31904247-G-T

50821429-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24086
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31902505-C-T

50821434-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24086
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31902503-T-A

50822497-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24086
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31901541-C-T

http://identifiers.org/hco/10/GRCh38#50822537-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24086
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#31901501-A-C

50822641-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24086
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31901397-A-G

50822816-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24086
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 31901224-G-A

50822816-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24086
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 31901224-G-T

50823356-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24086
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31900684-G-A

http://identifiers.org/hco/10/GRCh38#50823377-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24086
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#31900663-C-A

http://identifiers.org/hco/10/GRCh38#50823564-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24086
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#31900573-C-A

50823564-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24086
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 31900573-C-T

50823566-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24086
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 31900571-T-G

50823572-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24086
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 31900565-G-A

50823913-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24086
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31900229-G-A

50823956-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24086
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31900205-A-G

http://identifiers.org/hco/10/GRCh38#50824145-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24086
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#31900046-C-A

50824193-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24086
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31899956-A-G

50824225-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24086
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31899920-T-C

50824278-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24086
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31899866-C-T

50824324-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24086
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31899827-A-G

50824452-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24086
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31899713-G-A

http://identifiers.org/hco/10/GRCh38#50824485-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24086
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#31899677-C-A

50824945-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24086
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31899275-T-C

50825287-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24086
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31898950-T-G

50825905-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24086
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31898880-T-G

50826241-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24086
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31898593-C-T

50826321-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24086
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31898517-T-A

50828238-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24086
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 31898277-T-C

50828548-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24086
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31897969-A-G

50828549-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24086
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31897968-C-G

50828798-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24086
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31897736-G-A

50828824-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24086
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31897715-G-T

http://identifiers.org/hco/10/GRCh38#50828837-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24086
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#31897702-C-A

50828905-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24086
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31897633-G-A

http://identifiers.org/hco/10/GRCh38#50828909-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24086
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#31897629-C-A

50828909-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24086
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31897629-C-T

50829219-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24086
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31897263-T-C

50829340-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24086
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31897164-A-G

50829360-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24086
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31897142-G-A

50835519-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24086
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31895998-T-C

50835552-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24086
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31895975-G-T

50836027-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24086
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31895555-G-T

http://identifiers.org/hco/10/GRCh38#50836029-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24086
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#31895553-C-A

50836029-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24086
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31895553-C-T

http://identifiers.org/hco/10/GRCh38#50836052-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24086
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#31895536-C-A

50836052-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24086
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31895536-C-T

50836175-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24086
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 31895419-A-G

50836916-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24086
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31894979-G-A

50836943-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24086
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31894950-C-T

50838779-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24086
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31893973-G-A

50838904-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24086
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31893844-A-G

http://identifiers.org/hco/10/GRCh38#50838967-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24086
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#31893794-C-A

50838967-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24086
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31893794-C-T

50839037-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24086
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31893731-A-T

50839125-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24086
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31893647-T-A

50839219-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24086
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31893557-C-G

50839222-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24086
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31893554-T-C

http://identifiers.org/hco/10/GRCh38#50839297-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24086
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#31893481-C-A

50839360-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24086
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31893420-G-A

50839525-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24086
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31890753-G-A

50839528-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24086
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31890750-C-T

http://identifiers.org/hco/10/GRCh38#50839599-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24086
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#31890687-C-A

50840802-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24086
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31889654-T-G

50840850-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24086
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31889594-A-G

http://identifiers.org/hco/10/GRCh38#50840920-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24086
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#31889529-C-A

50840955-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24086
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31889492-A-G

50841423-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24086
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31889043-G-T

http://identifiers.org/hco/10/GRCh38#50841606-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24086
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#31888861-C-A

http://identifiers.org/hco/10/GRCh38#50841648-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24086
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#31888819-C-A

50841708-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24086
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31888773-A-T

50841777-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24086
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31888708-T-A

50841777-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24086
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31888708-T-G

50841818-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24086
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31888678-T-C

50841828-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24086
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31888668-G-A

50842045-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24086
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31888451-G-A

50842045-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24086
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31888451-G-T

50842046-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24086
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31888450-T-C

50842047-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24086
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31888449-A-G

http://identifiers.org/hco/10/GRCh38#50842070-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24086
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#31888425-C-A

50842070-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24086
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31888425-C-T

50842201-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24086
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31888244-G-T

50842774-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24086
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31887929-G-A

50842956-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24086
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31887678-C-G

50843008-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24086
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31887628-A-G

50843137-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24086
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31887499-C-G

50843137-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24086
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31887499-C-T

50843156-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24086
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31887480-C-T

50843495-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24086
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31887197-C-G

50843580-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24086
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31887107-G-A

50843629-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24086
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31887060-A-G

50843633-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24086
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31887056-C-T

50843635-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24086
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31887054-G-A

50843779-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24086
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31886907-G-A

50843811-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24086
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31886872-T-C

50843960-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24086
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31886591-A-G

50843970-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24086
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31886575-T-C

50844132-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24086
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31886180-C-T

50844175-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24086
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31886131-T-A

50844176-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24086
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31886130-T-A

50844176-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24086
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31886130-T-G

50844245-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24086
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31886056-T-A

50844245-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24086
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31886056-T-C

50844330-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24086
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31885977-A-G

50844703-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24086
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31884920-G-A

50844747-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24086
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31884876-A-G

50844819-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24086
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31884803-G-A

50844820-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24086
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31884802-T-C

http://identifiers.org/hco/10/GRCh38#50844909-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24086
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#31884709-C-A

50845010-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24086
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31884626-T-C

50845057-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24086
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31884579-A-G

50845070-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24086
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31884567-A-G

50845273-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24086
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31884389-T-C

50845288-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24086
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31884373-A-G

50845542-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24086
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31884122-G-A

50846046-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24086
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31883861-C-T

50846062-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24086
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31883845-T-C

50846464-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24086
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31883712-T-A

50846470-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24086
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31883706-T-C

50846489-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24086
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31883687-A-T

50846856-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24086
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 31883345-G-A

50847183-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24086
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31883033-G-T

50847228-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24086
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31882976-G-A

50847282-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24086
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31882914-A-G

50847540-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24086
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31882684-A-G

50847540-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24086
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31882684-A-T

50847797-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24086
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31882493-G-T

50850351-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24086
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31881137-T-C

50850598-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24086
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31880954-G-A

50850598-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24086
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31880954-G-T

50850652-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24086
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31880900-A-T

50850680-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24086
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 31880875-T-A

50850721-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24086
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 31880834-G-A

50850733-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24086
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 31880822-C-T

50850743-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24086
most severe consequence: intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 31880807-G-A

http://identifiers.org/hco/10/GRCh38#50850746-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24086
most severe consequence: intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#31880804-C-A

50850746-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24086
most severe consequence: intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 31880804-C-G

50850746-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24086
most severe consequence: intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 31880804-C-T

50850778-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24086
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 31880782-C-T

50850830-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24086
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31880734-C-G

50850830-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24086
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31880734-C-T

50850901-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24086
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31880671-A-G

50850901-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24086
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31880671-A-T

http://identifiers.org/hco/10/GRCh38#50850956-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24086
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#31879293-C-A

50850956-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24086
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31879293-C-T

50850988-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24086
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31879260-C-G

50851092-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24086
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31879158-G-A

http://identifiers.org/hco/10/GRCh38#50851327-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24086
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#31878951-A-C

50851327-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24086
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31878951-A-G

50851506-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24086
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31878758-T-G

50851531-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24086
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31878733-A-G

50851593-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24086
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31878638-A-G

http://identifiers.org/hco/10/GRCh38#50851628-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24086
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#31878600-A-C

50851692-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24086
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31878542-C-T

50851795-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24086
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31878454-G-T

50851987-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24086
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31878272-G-T

http://identifiers.org/hco/10/GRCh38#50852086-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24086
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#31878178-C-A

50852154-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24086
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31878109-G-A

50852205-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24086
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31878059-T-C

50852243-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24086
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31878024-A-G

50852250-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24086
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31878017-G-A

50852334-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24086
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31877938-C-T

50852338-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24086
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31877929-A-G

50852644-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24086
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31877680-A-G

50852950-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24086
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31875637-C-T

50853643-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24086
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31874907-C-T

50853884-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24086
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31874378-G-A

50855597-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24086
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31873667-T-C

50855616-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24086
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31873643-G-A

50855616-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24086
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31873643-G-T

50855917-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24086
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31873425-T-A

50856054-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24086
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31873322-T-A

50856246-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24086
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31873167-A-G

50856347-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24086
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31873054-C-G

50856365-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24086
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31872990-T-C

50858477-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24086
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31872206-C-T

50858755-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24086
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31871735-T-C

50858896-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24086
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31871531-A-G

50858964-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24086
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31871457-A-G

50859208-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24086
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31871212-T-A

50859239-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24086
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31871181-A-G

50859259-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24086
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31871161-A-G

50859345-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24086
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31871095-G-C

50859589-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24086
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31870848-G-A

50859768-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24086
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31870670-A-G

http://identifiers.org/hco/10/GRCh38#50859788-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24086
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#31870651-C-A

50859885-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24086
most severe consequence: 5_prime_UTR_variant, intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 31870553-G-C

http://identifiers.org/hco/10/GRCh38#50860076-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24086
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#31870366-C-A

50860087-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24086
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31870355-T-A

http://identifiers.org/hco/10/GRCh38#50860128-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24086
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#31870314-C-A

50862769-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24086
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31868869-G-T

http://identifiers.org/hco/10/GRCh38#50862770-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24086
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#31868868-C-A

50862822-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24086
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31868814-A-G

50862847-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24086
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31868787-T-A

50862915-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24086
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 31868724-T-C

50863121-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24086
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31868518-A-G

50864120-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24086
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31867558-A-G

50864233-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24086
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31867456-G-A

50864244-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24086
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31867443-T-C

50864287-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24086
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31867396-C-G

50864292-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24086
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31867364-G-C

50864467-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24086
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31866879-A-G

50865475-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24086
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31866422-T-A

50865622-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24086
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31866324-C-G

50865622-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24086
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31866324-C-T

50867982-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24086
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31865121-T-C

50868532-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24086
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31864528-T-C

50868607-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24086
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31864466-T-C

50868790-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24086
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31864312-T-A

50869644-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24086
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31864186-G-A

50869648-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24086
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31864182-T-C

50869855-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24086
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31863993-G-A

50870432-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24086
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31863674-G-A

http://identifiers.org/hco/10/GRCh38#50870499-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24086
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#31863615-A-C

50870983-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24086
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31862928-G-A

50871101-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24086
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31862808-A-G

50871101-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24086
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31862808-A-T

50871400-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24086
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31862551-T-C

50871548-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24086
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31862423-A-G

50871708-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24086
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31862262-G-A

50872106-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24086
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31861860-A-G

50872429-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24086
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31861297-G-A

50872429-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24086
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31861297-G-T

50873318-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24086
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31861129-A-T

50873395-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24086
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31861000-C-T

50873813-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24086
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31860607-A-T

50873879-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24086
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31860546-A-G

50874224-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24086
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31860190-A-G

50874440-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24086
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31859966-A-G

50874993-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24086
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31859339-T-C

50875200-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24086
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31859151-A-G

50875243-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24086
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31859109-G-A

50875411-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24086
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31858963-C-G

50875411-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24086
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31858963-C-T

50876447-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24086
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31858418-A-T

http://identifiers.org/hco/10/GRCh38#50877681-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24086
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#31856388-A-C

50878790-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24086
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31856106-C-G

50878927-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24086
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31855991-C-G

50879251-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24086
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31855711-T-C

50879268-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24086
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31855702-T-C

50879287-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24086
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31855683-A-G

50879845-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24086
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31855511-G-A

50880917-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24086
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31854527-G-A

50880964-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24086
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31854491-T-G

50881562-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24086
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31850778-A-G

50881612-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24086
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31850725-T-C

http://identifiers.org/hco/10/GRCh38#50881755-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24086
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#31850585-A-C

http://identifiers.org/hco/10/GRCh38#50882465-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24086
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#31849259-C-A

50882485-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24086
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31849239-G-C

50882623-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24086
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 31849100-G-A

50882653-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24086
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 31849070-T-C

50882738-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24086
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31848985-G-A

50882780-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24086
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31848944-G-C

50882851-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24086
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 31848872-A-G

50882894-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24086
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 31848832-T-C

50882894-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24086
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 31848832-T-G

http://identifiers.org/hco/10/GRCh38#50883016-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24086
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#31848694-C-A

50883016-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24086
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31848694-C-G

50883314-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24086
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31848453-T-C

50883465-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24086
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31848305-G-A

50883572-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24086
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31848196-T-G

50883632-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24086
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31848134-G-C

50883786-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24086
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31847988-G-A

50883786-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24086
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31847988-G-C

50883880-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24086
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31847900-T-C

50884110-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24086
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31847661-G-A

50884300-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24086
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31847503-G-T

50884456-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24086
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31847342-C-G

50884460-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24086
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31847338-C-G

50884605-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24086
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31847196-A-G

50884724-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24086
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31847090-T-C

50884920-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24086
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31846897-C-T

50885029-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24086
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31846784-T-C

50885100-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24086
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31846712-T-A

50885136-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24086
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31846677-G-T

50885380-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24086
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31846460-C-T